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中文
ENU诱导在 intron 13 的 splice donor site 处由 T 转换为 C 的点突变。RT-PCR 验证了全长转录本的缺失以及两个较短产物的产生。预测的截短蛋白会丢失 C 尾端的 770 个氨基酸，包括激酶区域。（来源：J:226897）
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
